SCA13

Introduction: SCA13

Description of SCA13

SCA13 (medical condition): A rare genetic disorder (chromosome 19 defect) characterized by...more »

See also:

Spinocerebellar ataxia 13:
  »Introduction: Spinocerebellar ataxia 13
  »Symptoms of Spinocerebellar ataxia 13

SCA13: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

SCA13 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that SCA13, or a subtype of SCA13, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

SCA13 as a Disease

SCA13: Another name for Spinocerebellar ataxia 13 (or close medical condition association).
  »Introduction: Spinocerebellar ataxia 13
  »Symptoms of Spinocerebellar ataxia 13

SCA13: Related Diseases

SCA13: SCA13 is listed as a type of (or associated with) the following medical conditions in our database:

• Degenerative conditions
• Brain conditions
• Head conditions
• Nervous system conditions
• Coordination and balance conditions
• Movement conditions
• Spinal cord conditions
• Back conditions
• Neuromuscular conditions
• Muscle conditions
• Genetic conditions
• Musculoskeletal conditions

Symptoms of SCA13 (Spinocerebellar ataxia 13)

Some of the symptoms of SCA13 incude:

• Gait ataxia
• Mild mental retardation
• Nystagmus
• Dysarthria
• Abnormal gait

See full list of 11 symptoms of SCA13 (Spinocerebellar ataxia 13)

SCA13: Related Disease Topics

These medical disease topics may be related to SCA13:

• progressive neurodegenerative disease
• genetic disorder
• Machado-Joseph disease
• nystagmus
• ataxia
• seizures
• hand tremor
• macular degeneration

Terms associated with SCA13:

Terms Similar to SCA13:

• Spinocerebellar ataxia 13
• Autosomal dominant cerebellar ataxia with mental retardation
• Cerebellar ataxia, autosomal dominant with mental retardation

Source - NIH

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